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Variant (rsID / SNP)

rs368923696

STK11

rs368923696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STK11. Location: chromosome 19, position 1,218,510. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

STK11Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:1218510
Cytoband
19p13.3
HGVS
NM_000455.5(STK11):c.374+11C>T
Allele change
Silent

Associated conditions / phenotypes

Peutz-Jeghers syndrome|Hereditary cancer-predisposing syndrome|Malignant tumor of breast

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.